US20090269851A1 - Use of disk surface for electroporation of adherent cells - Google Patents

Use of disk surface for electroporation of adherent cells Download PDF

Info

Publication number
US20090269851A1
US20090269851A1 US12/425,141 US42514109A US2009269851A1 US 20090269851 A1 US20090269851 A1 US 20090269851A1 US 42514109 A US42514109 A US 42514109A US 2009269851 A1 US2009269851 A1 US 2009269851A1
Authority
US
United States
Prior art keywords
disk
cells
vessel
electrodes
electrode
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/425,141
Other languages
English (en)
Inventor
Charles W. Ragsdale
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bio Rad Laboratories Inc
Original Assignee
Bio Rad Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bio Rad Laboratories Inc filed Critical Bio Rad Laboratories Inc
Priority to US12/425,141 priority Critical patent/US20090269851A1/en
Publication of US20090269851A1 publication Critical patent/US20090269851A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M25/00—Means for supporting, enclosing or fixing the microorganisms, e.g. immunocoatings
    • C12M25/06—Plates; Walls; Drawers; Multilayer plates
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M35/00—Means for application of stress for stimulating the growth of microorganisms or the generation of fermentation or metabolic products; Means for electroporation or cell fusion
    • C12M35/02—Electrical or electromagnetic means, e.g. for electroporation or for cell fusion

Definitions

  • This invention lies in the field of transfection, the process by which exogenous molecular species are inserted into membranous structures by rendering the membrane permeable on a transient basis while the structures are in contact with a liquid solution of the species, thereby allowing the species to pass through the membrane, and doing so in such a manner that the structures resume their viability after the procedure is complete.
  • exogenous species including hydrophilic or membrane-impermeant species
  • a high efficiency transfection is one in which the exogenous species has entered a high proportion of the cells or a population being treated and the viability of the cells has either been maintained throughout or restored after the procedure.
  • electroporation which is the use of an electric field as the source of energy for the membrane permeabilization, has received the most attention.
  • Transfection has been performed both on cells that are suspended in a buffer solution and on adherent cells, i.e, cells that are immobilized on a solid surface which is often the surface on which the cells have been grown. Achieving high efficiency is a continuing challenge in all forms of electroporation, but even more so in the electroporation of adherent cells. Disclosures of electroporation of adherent cells are found in the following published documents:
  • the cells to be transfected in accordance with this invention are grown or otherwise immobilized on the substantially flat surface of a circular disk in the area between the periphery of the disk and an inner circle within and concentric with the periphery.
  • the cells thus occupy the surface of a flat ring.
  • a cylinder with electrode material in the form of an electrode or a series of electrodes on its convex outward-facing surface and with a diameter that is equal to or less than the diameter of the inner circle serves as an inner electrode.
  • a second, hollow cylinder with electrode material in the form of an electrode or series of electrodes on its concave inner surface encircles the periphery of the disk to serve as the outer electrode.
  • the liquid solution of the exogenous species, referred to herein as the “transfecting species,” that will enter the cells is retained in a vessel that is large enough to receive both the disk and the electrodes with the disk surface immersed in the solution.
  • the cylinder supporting the outer electrode(s) can itself serve as the vessel, with the outer electrodes on the inward-facing surface of the vessel.
  • the two electrodes (or series of electrodes) and the inner and outer electrodes are supported in the vessel in such a manner that the cells lie in a plane at the disk surface and the inner and outer electrodes both traverse the plane.
  • the cylindrical surfaces on which the inner and outer electrodes reside form coaxial cylinders with a common cylinder axis, and the surface of the disk on which the cells reside is placed is transverse, and preferably perpendicular, to the axis.
  • the electrodes when activated thus produce an electric field across the surface of the flat ring, exposing the cells on the surface to the field.
  • the inner electrode material resides on an outward-facing surface of a cylindrical support, and in certain embodiments of the invention, the disk and this cylindrical support with the inner electrode(s) on its surface are rigidly joined to form a unitary member.
  • the disk and the inner cylinder are separate components of the apparatus allowing cells to be grown on the disk surface without the presence of the inner cylinder. Regardless of whether the disk is integrated with the inner cylinder or separate, it is preferred that the disk be readily removable from the outer cylinder so that cells can be grown on the disk surface outside the apparatus.
  • a disk that is removable from the outer cylinder offers flexibility and efficiency to the procedure by allowing cells to be grown on, or otherwise adhered to, one disk while cells on another disk are being subjected to electroporation.
  • the disk can be placed in a vessel that allows the disk, or two or more disks, to be rotated while cells are being grown on its surface.
  • the rotation agitates the surrounding growth medium and thereby improves access of the cells to the nutrients in the medium and to gases that promote cell growth.
  • the disk can also be rotated inside the electroporation chamber (i.e., the outer cylinder) during electroporation.
  • the electrode material on the outer wall of the inner cylinder extends around the full circumference of the inner cylinder to form a continuous lining
  • this electrode material forms a patch or narrow strip affixed to the surface of the inner cylinder at a point on, or along a relatively short segment of, the circumference, or a series of patches or narrow strips distributed around the circumference, preferably with a uniform spacing.
  • the electrode material forming the outer electrode is either a continuous lining extending around the full circumference of the outer cylinder, a patch or strip, or a series of patches or strips to correspond to those on the inner cylinder.
  • the disk in preferred embodiments is designed to be rotatable relative to both cylinders and hence to the electrodes, thereby allowing segments of the disk surface in succession to be placed in the space between the electrodes.
  • a small gap is maintained between the inner edge of the disk and the inner electrode, or between the outer edge of the disk and the outer electrode, or both.
  • the gaps when present will avoid the formation of electric field anomalies at the edges of the disk.
  • the inner and outer electrodes preferably extend both above and below the disk surface.
  • a buffer solution containing the exogenous species is placed in the cylindrical receptacle formed by the outer cylinder with both electrodes in electrical contact with the solution and with the adherent cells immersed in the solution. The solution thus extends above the disk surface on which the cells reside, requiring no more than a shallow depth of liquid above the cells.
  • FIG. 1 a is a side view of an integrated disk and inner cylinder for use in the present invention.
  • FIG. 1 b is a top view of the integrated disk and inner cylinder of FIG. 1 a.
  • FIG. 2 is a cross section of a vessel with the integrated disk and inner cylinder of FIGS. 1 a and 1 b placed inside the vessel, and a solution of transfecting species covering the disk surface.
  • FIG. 3 a is a top view of an alternative disk for sue in the present invention.
  • FIG. 3 b is a vertical cross section of the disk of FIG. 3 a.
  • FIG. 4 is a cross section of a vessel with the disk of FIGS. 3 a and 3 b placed inside the vessel, together with an inner cylinder an a solution of transfecting species.
  • FIG. 5 is a diagram of a vessel for growing cells on several disks of the type shown in FIGS. 3 a and 3 b.
  • FIG. 6 is a top view of an inner and outer cylinder combination containing an alternative electrode arrangement, still within the scope of the invention.
  • FIG. 7 is a circuit diagram for the electrodes of FIG. 6 .
  • the width of the ring-shaped area between the two cylindrical surfaces and on which the adherent cells reside is preferably small compared to the outer diameter of the disk so that the intensity of the electrical field created by the electrodes varies only minimally in the radial direction across the cell area when the electrodes fully extend around the circumferences of their respective cylinders.
  • the ratio of the diameter of the inner edge to the diameter of the outer edge is preferably within the range of about 0.2 to about 0.95, more preferably the range of about 0.3 to about 0.9, and most preferably the range of about 0.5 to about 0.8.
  • the gap will provide room to allow the user to readily insert the disk, the inner cylinder, or an integrated disk and inner cylinder, into the outer cylinder and to remove it when desired.
  • the gap is preferably small enough however to accommodate as wide a disk as possible and to thereby make maximal use of the distance between the electrodes for transfection of the cells.
  • a gap width within the range of about 30 microns to about 3 mm, more preferably the range of about 100 microns to about 1 mm, will be useful.
  • the distance between electrodes facing each other across the width of the ring-shaped area on the disk can vary with the needs of the cells that are being transfected, although best results in most cases will be obtained with a distance in the range of about 0.3 cm to about 10 cm.
  • the disk surface can be fabricated of any material that is capable of serving as an immobilizing support for the cells.
  • suitable materials are glass, polycarbonate, polystyrene, polyvinyl, polyethylene, and polypropylene.
  • Microporous membranes used in membrane-based cell culture can also be used. Examples are membranes of hydrophilic poly(tetrafluoroethylene), cellulose esters, polycarbonate, and polyethylene terephthalate.
  • a membrane that is otherwise flexible can be maintained flat by placing the membrane over a rigid material such as a rigid screen or a glass or polymeric disk.
  • adherence of the cells to the surface can be achieved by conventional means, including the inherent adherence when the cells are grown on the surface, as well as adherence through immunological or affinity-type binding, electrostatic attraction, or covalent coupling.
  • the electrodes can be formed of electrode materials that are conventionally used in electroporation.
  • the inner electrode can constitute the entire inner cylinder, which can either be of solid electrode material or hollow, and the outer electrode can likewise constitute the entire side wall of the chamber in which the ring, the inner electrode, and the buffer solution are retained.
  • either or both of the inner and outer electrodes can be formed as surface layers, patches, or strips over electrically insulating materials.
  • An electrically insulating cylindrical core for example, can be plated on its outer surface with a metallic material to form the inner electrode, and an insulating shell can likewise be plated on its inner surface with a metallic material to form the outer electrode.
  • the disk In use, the disk will be centered in the apparatus.
  • centering can be accomplished by any of various features.
  • a centering feature is a knob, or protrusion in general, at the underside of the disk, to mate with an indentation(s) in the floor of the chamber that is formed by the outer cylinder.
  • the protrusion can be centered on the underside of the inner cylinder.
  • the protrusion(s) can extend upward from the floor of the chamber to mate with an indentation in the underside of the inner cylinder.
  • two or more protrusions or indentations can be arranged on the underside of the disk outside of the central opening of the disk.
  • a single circular ridge (or circular groove) mated with a complementary groove (or ridge) will serve the same function. Still further variations will be readily apparent, including those shown in the Figures and described below.
  • Centering of the inner cylinder itself, independently of the disk or with the disk attached, is likewise of value in certain embodiments of the invention.
  • the centering features described above will serve the purpose, and when the cylinder and the disk are separate, the cylinder can be supported from the top of the chamber with a centering feature.
  • a further example of a centering feature that is integrated into the floor of the chamber and engages either the disk, the inner cylinder, or both is a magnet on one part and a facing insert of ferrous metal or other magnetically responsive material on the other.
  • a magnet can thus be bonded or molded into the floor of the chamber, to attract a magnetically responsive metal bead, ball, or chip in the disk or the inner cylinder along the underside thereof, or vice versa.
  • a magnet or magnetically active metal in a knob extending from the base of the disk or the inner cylinder when the disk is mounted to the inner cylinder.
  • centering features are support brackets, a flange, or a shoulder extending from the inner cylinder, the outer cylinder, or both.
  • the amount of the solution that is placed inside the chamber to contact the disk and cells adherent to the disk surface is not critical, but an advantage of this invention is that it allows one to use a very thin or shallow layer of the solution over the cells, and to thereby concentrate the electrical field over and around the cells.
  • An amount of solution that is just enough to cover the cells can be used, and in general, the depth above the cells will preferably range from about 0.5 mm to about 5 mm.
  • Biological cells that can be transfected by the present invention include those that are grown on the disk surface and are naturally adherent thereto and those whose adherence is enhanced by cell-adhesive molecules that are either coupled to the cells or to the surface. All such cells are referred to herein as “adherent cells.” Examples of adherent cells are neuronal cells, neuronal stem cells, mesenchymal stem cells, pancreatic cells, skeletal muscle cells, cardiomyocytes, and liver or liver-derived cells such as primary hepatocytes, liver epithielial cells, HepG2 cells, and hepatocellular carcinoma-derived cells.
  • transfecting species to be inserted into the cells by the present invention are nucleic acids including DNA, RNA, plasmids, and genes and gene fragments, as well as proteins, pharmaceuticals, and enzyme cofactors. Further examples will be apparent to those skilled in the art.
  • FIGS. 1 a and 1 b are two views of an integrated disk and inner cylinder 11 , FIG. 1 a showing the component from the side and FIG. 1 b showing a top view.
  • the disk 12 has a flat upper surface 13 bounded on the inside by the cylinder 14 and on the outside by a circular perimeter edge 15 , the cylinder 14 and the perimeter edge 15 being concentric or coaxial.
  • the cylinder 14 is either constructed of a continuous electrode material or of a core of non-electrode material with a layer of electrode material on its outer surface, in either case with an appropriate electrical connection between the electrode material and a power source (not shown).
  • a knob 16 protrudes downward from the underside of the cylinder 14 at the center, and is shown as a small cylinder in these Figures but can also assume a variety of other shapes, including a hemisphere.
  • the knob 16 is a centering feature and mates with an indentation of complementary shape in the floor of the chamber that is formed by the outer cylinder which is shown in FIG. 2 .
  • the centering feature can also include a magnet or a magnetically responsive metal, as discussed below.
  • the knob 16 can also serve as the electrical connection that supplies power to the electrode, together with an electrical contact in the indentation to complete the circuit.
  • FIG. 2 shows the integrated disk and inner cylinder 11 of FIGS. 1 a and 1 b in position inside the chamber 21 .
  • the chamber 21 which is shown in cross section, is constructed of a cylindrical side wall 22 and a flat base 23 , and in this particular example is open at the top.
  • Electrode material constitutes either the entire side wall 22 of the cylinder or a layer on the inner surface 24 of the cylinder, with an appropriate electrical connection between the electrode material and the power source.
  • the dimensions of the cylindrical wall 22 and the disk 12 are such that a small gap 25 exists between inner surface 24 of the side wall and the outer edge 15 of the disk.
  • the central unit i.e., the integrated disk and inner cylinder
  • the cylindrical knob 16 of FIGS. 1 a and 1 b is replaced by a hemispherical knob 26 that fits into a hemispherical indentation 27 in the flat base 23 of the chamber.
  • Cells 28 into which the exogenous molecular species are to be inserted adhere to the upper surface of the ring 12 , and the solution 29 containing the exogenous species covers the cells.
  • the knob 26 contains magnetically responsive metal, and a magnet 31 is attached to the underside of the chamber by way of a removable support such as a sliding strip.
  • FIGS. 3 a and 3 b depict an alternative type of disk 32 that is separate from the inner cylinder.
  • FIG. 3 a is a top view of the disk and
  • FIG. 3 b is a side view in cross section.
  • the surface 33 of this disk to which the cells adhere is of the same shape as, or a shape similar to, that of the surface of the disk in the preceding Figures, but the disk in FIGS. 3 a and 3 b has an exposed inner edge or rim 34 in addition to its exposed outer edge or periphery 35 , the inner edge surrounding a central opening 36 .
  • a centering feature in the form of a hemispherical knob 37 protrudes from a bracket 38 extending downward from the disk.
  • the bracket 38 is shown as a hollow hemisphere but can alternatively be a basket-type structure or a series of curved spokes.
  • FIG. 4 shows the disk 32 of FIGS. 3 a and 3 b inserted in a chamber 41 .
  • the chamber 41 in FIG. 4 which is likewise shown in cross section, has a cylindrical side wall 42 and a flat base 43 , with an indentation 44 in the base that is complementary in contour to the knob 37 protruding from the disk bracket 38 , and with an electrode layer 45 on the inner surface of the side wall.
  • An inner cylindrical electrode 46 is mounted to a lid 47 that rests on the top of the cylindrical side wall 42 and extends into the chamber interior and through the central opening 36 of the disk 32 .
  • the central opening 36 is wide enough to leave a small gap 48 between the inner cylinder and the disk.
  • the gap 48 permits easy insertion and removal of the inner cylinder 46 , and reduces or eliminates electric field anomalies at the inner edge of the disk.
  • FIGS. 1 a, 1 b, 2 , 3 a, 3 b, and 4 depicts a knob attached to the disk.
  • the knob When the knob is magnetized or contains a magnetically responsive material, the disk can be rotated by a motorized rotating magnet, either in the chamber or in a separate vessel. Rotation of the disk in a separate vessel containing a growth medium offers a means of facilitating the growth of cells on the disk surface.
  • FIG. 5 An example of such a vessel is shown in FIG. 5 .
  • the vessel 51 in FIG. 5 accommodates several disks 52 , or several units consisting of cylinders with integrated disks.
  • the vessel 51 is filled with a liquid nutrient medium 53 and contains a source of nutrient gas 54 such as carbon dioxide.
  • Beneath the floor 55 of the vessel are a series of rotary motors 56 each with a magnetic member 57 .
  • the rotating magnetic field produced by a rotating motor causes rotation of the disk whose protruding magnetic knob is in the magnetic field.
  • the rotation enhances the access of the cells on the disk surface to the nutrients in the medium 53 and to the gas 54 .
  • FIG. 6 is an example of an apparatus in which series of discrete electrodes are used for both the inner and outer electrodes, the electrodes in each individual series being distributed around the full circumference of the cylinder on which the series is formed, and evenly spaced within each series.
  • FIG. 6 shows the inner cylinder 61 and the outer cylinder 62 .
  • a first series of strip electrodes 63 is secured to the outer surface of the outer cylinder 62 while a second series of strip electrodes 64 is secured to the outer surface of the inner cylinder 61 .
  • the two series are complementary, together forming pairs of electrodes facing each other across the space between the two cylinders.
  • the disk is not shown, its construction and means of centering can be the same as those shown in the preceding Figures.
  • the electrodes can all be energized or pulsed simultaneously, or opposing pairs can be energized in succession around the disk. When pairs are individually energized, the resulting electric field will extend over cells occupying a wedge-shaped segment of the disk surface.
  • a circuit for controlling the electrodes is shown in FIG. 7 in which circuit connections for only three electrode pairs 63 a / 64 a, 63 b / 64 b, 63 c / 64 c, are shown for simplicity, the remaining connections being understood.
  • a controller 71 controls a series of pairs of bipolar transistors 72 / 72 ′, 73 / 73 ′, 74 / 74 ′ corresponding with the individual electrode pairs in accordance with a selected protocol.
  • the series of electrode pairs can also be replaced with a single electrode pair, i.e., one pair of the opposing strip electrodes shown in FIG. 6 , and a rotating mechanism can be incorporated in the chamber to rotate the disk in increments to expose successive segments of the disk surface to the electric field pulses.

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical & Material Sciences (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Sustainable Development (AREA)
  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Cell Biology (AREA)
  • Immunology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Plant Pathology (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
US12/425,141 2008-04-24 2009-04-16 Use of disk surface for electroporation of adherent cells Abandoned US20090269851A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/425,141 US20090269851A1 (en) 2008-04-24 2009-04-16 Use of disk surface for electroporation of adherent cells

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US4763708P 2008-04-24 2008-04-24
US12/425,141 US20090269851A1 (en) 2008-04-24 2009-04-16 Use of disk surface for electroporation of adherent cells

Publications (1)

Publication Number Publication Date
US20090269851A1 true US20090269851A1 (en) 2009-10-29

Family

ID=41215400

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/425,141 Abandoned US20090269851A1 (en) 2008-04-24 2009-04-16 Use of disk surface for electroporation of adherent cells

Country Status (5)

Country Link
US (1) US20090269851A1 (fr)
EP (1) EP2269031A4 (fr)
JP (1) JP2011518561A (fr)
CA (1) CA2721719A1 (fr)
WO (1) WO2009131972A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011153164A1 (fr) * 2010-06-03 2011-12-08 The Regents Of The University Of California Configuration d'électrodes d'électroporation et méthodes afférentes
US20130189771A1 (en) * 2012-01-25 2013-07-25 Hans Strandberg Cell culture device
US9382510B2 (en) 2011-08-25 2016-07-05 Jian Chen Methods and devices for electroporation

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2399984B1 (fr) 2010-06-22 2013-03-20 Lonza Cologne GmbH Procédé et agencement d'électrodes pour le traitement de cellules adhérentes

Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4882281A (en) * 1986-04-02 1989-11-21 Jeffrey L. Hilliard Probe for electrofusion, electroporation, or like procedure
US5128257A (en) * 1987-08-31 1992-07-07 Baer Bradford W Electroporation apparatus and process
US5134070A (en) * 1990-06-04 1992-07-28 Casnig Dael R Method and device for cell cultivation on electrodes
US5232856A (en) * 1990-06-25 1993-08-03 Firth Kevin L Electroporation device
US5304486A (en) * 1987-10-09 1994-04-19 Baylor College Of Medicine Method of and apparatus for cell portion and cell fusion using radiofrequency electrical pulse
US5422272A (en) * 1993-07-14 1995-06-06 Andrew A. Papp Improvements to apparatus and method for electroporation
US5964726A (en) * 1994-02-25 1999-10-12 Ramot University Authority For Applied Research And Industrial Development Apparatus and method for efficient incorporation of molecules into cells
US6001617A (en) * 1989-06-07 1999-12-14 Queen's University At Kingston Electroporation device and method of use
US6261815B1 (en) * 1996-09-23 2001-07-17 Duke University Method of introducing exogenous compounds into cells by electroporation and apparatus for same
US20030148524A1 (en) * 2002-01-21 2003-08-07 Ulrich Zimmermann Method and device for electroporation of biological cells
US20040029240A1 (en) * 2002-05-13 2004-02-12 Acker Jesse L. Dynamic electroporation apparatus and method
US20040235150A1 (en) * 2001-04-17 2004-11-25 Takao Takagi Cell and strucuture incubator
US20050070018A1 (en) * 2003-09-30 2005-03-31 Lee Johnson Microelectronic cell electroporation array
US6897069B1 (en) * 2004-06-08 2005-05-24 Ambion, Inc. System and method for electroporating a sample
US20050170510A1 (en) * 2003-12-08 2005-08-04 Yong Huang Device and method for controlled electroporation and molecular delivery into cells and tissue
US20070031816A1 (en) * 2003-12-15 2007-02-08 P.A.L.M. Microlaser Technologies Ag Mounting device for mounting a retainer means for a biological object and corresponding method for laser micro-dissection
US20070125942A1 (en) * 2005-07-06 2007-06-07 The Regents Of The University Of California Apparatuses, systems and methods for isolating and separating biological materials
US20070155016A1 (en) * 2004-03-12 2007-07-05 The Regents Of The University Of California Method and apparatus for integrated cell handling and measurements

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0460099U (fr) * 1990-09-27 1992-05-22
AU2002230999A1 (en) * 2000-12-21 2002-07-01 Medtronic, Inc. Electrically responsive promoter system
AU2004280029B2 (en) * 2003-10-08 2009-02-26 Kyoto University Method of introducing nucleic acid
JP2005261323A (ja) * 2004-03-19 2005-09-29 National Institute Of Advanced Industrial & Technology エレクトロポレーションによる遺伝子導入法
JP2006006136A (ja) * 2004-06-23 2006-01-12 Teijin Ltd 細胞培養器
JP2007167002A (ja) * 2005-12-22 2007-07-05 Asahi Techno Glass Corp 細胞培養用カセット、細胞培養用カセット着脱用治具及び細胞培養装置
US7799555B2 (en) * 2006-02-10 2010-09-21 Bio-Rad Laboratories, Inc. Apparatus for high-throughput electroporation

Patent Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4882281A (en) * 1986-04-02 1989-11-21 Jeffrey L. Hilliard Probe for electrofusion, electroporation, or like procedure
US5128257A (en) * 1987-08-31 1992-07-07 Baer Bradford W Electroporation apparatus and process
US5304486A (en) * 1987-10-09 1994-04-19 Baylor College Of Medicine Method of and apparatus for cell portion and cell fusion using radiofrequency electrical pulse
US6001617A (en) * 1989-06-07 1999-12-14 Queen's University At Kingston Electroporation device and method of use
US5134070A (en) * 1990-06-04 1992-07-28 Casnig Dael R Method and device for cell cultivation on electrodes
US5232856A (en) * 1990-06-25 1993-08-03 Firth Kevin L Electroporation device
US5422272A (en) * 1993-07-14 1995-06-06 Andrew A. Papp Improvements to apparatus and method for electroporation
US5964726A (en) * 1994-02-25 1999-10-12 Ramot University Authority For Applied Research And Industrial Development Apparatus and method for efficient incorporation of molecules into cells
US6261815B1 (en) * 1996-09-23 2001-07-17 Duke University Method of introducing exogenous compounds into cells by electroporation and apparatus for same
US20040235150A1 (en) * 2001-04-17 2004-11-25 Takao Takagi Cell and strucuture incubator
US20030148524A1 (en) * 2002-01-21 2003-08-07 Ulrich Zimmermann Method and device for electroporation of biological cells
US20040029240A1 (en) * 2002-05-13 2004-02-12 Acker Jesse L. Dynamic electroporation apparatus and method
US20050070018A1 (en) * 2003-09-30 2005-03-31 Lee Johnson Microelectronic cell electroporation array
US20050170510A1 (en) * 2003-12-08 2005-08-04 Yong Huang Device and method for controlled electroporation and molecular delivery into cells and tissue
US20070031816A1 (en) * 2003-12-15 2007-02-08 P.A.L.M. Microlaser Technologies Ag Mounting device for mounting a retainer means for a biological object and corresponding method for laser micro-dissection
US20070155016A1 (en) * 2004-03-12 2007-07-05 The Regents Of The University Of California Method and apparatus for integrated cell handling and measurements
US6897069B1 (en) * 2004-06-08 2005-05-24 Ambion, Inc. System and method for electroporating a sample
US20070125942A1 (en) * 2005-07-06 2007-06-07 The Regents Of The University Of California Apparatuses, systems and methods for isolating and separating biological materials

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011153164A1 (fr) * 2010-06-03 2011-12-08 The Regents Of The University Of California Configuration d'électrodes d'électroporation et méthodes afférentes
CN102985132A (zh) * 2010-06-03 2013-03-20 加利福尼亚大学董事会 电穿孔电极构造和方法
US9382510B2 (en) 2011-08-25 2016-07-05 Jian Chen Methods and devices for electroporation
US11959061B2 (en) 2011-08-25 2024-04-16 Jian Chen Methods and devices for electroporation
US20130189771A1 (en) * 2012-01-25 2013-07-25 Hans Strandberg Cell culture device

Also Published As

Publication number Publication date
WO2009131972A1 (fr) 2009-10-29
CA2721719A1 (fr) 2009-10-29
EP2269031A4 (fr) 2011-11-30
EP2269031A1 (fr) 2011-01-05
JP2011518561A (ja) 2011-06-30

Similar Documents

Publication Publication Date Title
EP1551948B1 (fr) Systeme de bioreacteur
CN104619830B (zh) 用于细胞培养的装置和方法
US20090269851A1 (en) Use of disk surface for electroporation of adherent cells
JP5674953B2 (ja) 細胞培養インサート
US7022518B1 (en) Apparatus and method for co-culturing of cells
JPH06189741A (ja) 細胞培養物インサート
JPH08173145A (ja) 膜を介する細胞の同時培養用のローラ瓶及びそれを使用する細胞の同時培養方法
KR20150013471A (ko) 교류 이온 자기 공명(ａｉｍｒ) 멀티-챔버-배양 장치 및 사용 방법
US9534206B2 (en) Cell carrier, associated methods for making cell carrier and culturing cells using the same
US10907125B2 (en) Flow through electroporation modules and instrumentation
JP2013529463A (ja) 接着細胞を均一に処理するための方法及び装置
US20230374432A1 (en) Bioreactor systems and methods for culturing cells
JPH0775553A (ja) 生体外で組織培養物を成長させる装置
US5470743A (en) Transmembrane cell culture device
US11225674B2 (en) Electroporation modules and instrumentation
JP5857309B1 (ja) 液滴形成用シャーレ及びそれを用いた電界撹拌方法
WO2010038013A1 (fr) Récipient de culture de cellules
US20090305380A1 (en) Electroporation of adherent cells with an array of closely spaced electrodes
JP2772656B2 (ja) 細胞等多重型培養装置
CN211999756U (zh) 一种分子生物实验用培养皿
CN212152307U (zh) 一种微生物培养皿
CN110804548B (zh) 一种细胞共培养设备
JP2014168397A (ja) 遠心分離機
US20100297753A1 (en) Transfection by laser poration on rotating cylinder
US20220169985A1 (en) Cell activation reactor and cell activation method

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION